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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 107 (1976), S. 51-65 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Mercuric-EDTA dehydrogenation of 2-substituted 1,3-diphenylimidazolidines gives normally the title compounds. Some exceptions leading to carbene intermediates are described and mechanisms are formulated.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 108 (1977), S. 273-278 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract From the hydroxylaminomethylation product of 2-naphthol (3) and aliphatic resp. aromatic aldehydes resulting compounds were examined by NMR spectroscopy. In solution the products of formaldehyde, acetaldehyde and benzaldehyde show equilibria of cyclic hydroxylamine and hydroxynitrone forms2 resp.1, the state of which depends on the solvent; with the derivatives of p-nitro- and p-dimethylaminobenzaldehyde only the hydroxynitrone form1 d resp.1 e is detectable.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 109 (1978), S. 1295-1303 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The structures of the title compounds are examined by13C-NMR and ESCA spectroscopy. Every double salt shows O-protonation, the proton lying within the experimental error half-way between the carbonyl oxygen atoms of the two molecules of amides resp. vinylogous amides.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 111 (1980), S. 627-633 
    ISSN: 1434-4475
    Keywords: Enaminones ; Mercury EDTA Dehydrogenation ; Neighbouring Effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Neighbouring effects during mercuryEDTA dehydrogenation yield with1 the vinylogous acylamidinium compound11 and with2, 3 and6 the vinylogous amidinium derivatives8–10.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 112 (1981), S. 1417-1423 
    ISSN: 1434-4475
    Keywords: Aminoalkylation ; Enaminones ; Tetrahydro-indeno-pyridines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The reaction of 1,3-indandione, formaldehyde and primary amines does not gives doubleMannich bases as described in literature, but the title compounds.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 118 (1987), S. 477-483 
    ISSN: 1434-4475
    Keywords: α-Iminium-ketone-oximes ; Mercuric EDTA dehydrogenation ; Anellated tetrahydro-β-carbolines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract 2-(Phenacyl)-tetrahydro-β-carboline (2) was transformed to theE/Z-oximes3 and4 and the isolated species cyclodehydrogenated to the nitrone5 and oxadiazine6. These compounds were dehydrated in acidic medium to the imidazole9.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 2475-2482 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: A New Method for the Preparation of 1.2-Dicarbonyl CompoundsThe dehydrogenation of α-aminoketones with mercuric acetate or mercuric complexes gives 1.2-dicarbonyl compounds in mostly good yields.
    Notes: Die Dehydrierung von α-Aminoketonen mit Quecksilber(II)-acetat bzw. Quecksilber(II)-Komplexen führt in meist guten Ausbeuten zu 1.2-Dicarbonylverbindungen.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 2485-2490 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Constitution of the Mannich Base from 2-Naphthol and HexamethylenetetramineThe product described by Galimberti und Erba has been incorrectly formulated as bis(2-naphthyloxymethyl)amine (2), it represents 1-(2,3-dihydro-1H-naphth[1,2-e][1,3]oxazin-2-ylmethyl)-2-naphthol (7).
    Notes: Das von Galimberti und Erba beschriebene Umsetzungsprodukt besitzt nicht die angegebene Konstitution eines Bis(2-naphthyloxymethyl)amins (2), sondern ist 1-(2,3-Dihydro-1H-naphth[1,2-e][1,3]oxazin-2-ylmethyl)-2-naphthol (7).
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  • 9
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Application of High-Resolution Solid State NMR Spectroscopy for the Determination of the Ring-Chain TautomerismThe structure of the benzaldehyde derivatives 1 and 2 showing ring-chain tautomerism was investigated by NMR spectroscopy in the solid state and in solution. Difficulties in preparing single crystals, low solubility, and the presence of solvent in the crystal prevent an X-ray analysis and other spectroscopic methods. The structural problem was solved by C-13 CP-MAS NMR spectroscopy. 2-[2-(Methylamino)ethyl]-3-nitrobenzaldoxime (1) exists in the chain form in the crystal but is in equilibrium with the cyclic isomer in solution. Two different types of crystals were obtained from the aminoethenylbenzaldehyde derivative 2, one of them containing the chain the other the cyclic form of 2. Signal assignments in the solid state result from comparison with the spectra in solution, which have been partially assigned by 2D 1H 13C NMR shift correlation.
    Notes: Die Struktur der Benzaldehyd-Derivate 1 und 2, die Ring-Ketten-Tautomerie zeigen, wird durch NMR-Spektroskopie im festen und gelösten Zustand untersucht. Schwierigkeiten beim Züchten von Einkristallen sowie die Schwerlöslichkeit bzw. die Anwesenheit von Kristallösungsmittel verhinderten die Anwendung der Röntgenstrukturanalyse und anderer spektroskopischer Methoden. Mit Hilfe von C-13-CP-MAS-NMR-Spektren wird das Strukturproblem lösbar. In 2-[2-(Methyl-amino)ethyl]-3-nitrobenzaldoxim (1) liegt im Kristall die offene Form vor, die in Lösung mit dem cyclischen Tautomeren 1b im Gleichgewicht steht. Vom Aminoethenylbenzaldehyd-Derivat 2 lassen sich zwei verschiedene Kristalle gewinnen, in denen alternativ die offene und die cyclische Struktur vorliegt. Zur Signalzuordnung werden die Festkörper-NMR-Spektren mit den z. T. durch 2D-1H-13C-NMR-Verschiebungskorrelation zugeordneten C-13-Spektren verglichen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1478-1489 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pyridones, III. Influence of Substituents on the Oxidation of Quaternary Pyridinium CompoundsBy hexacyanoferrate(III) oxidation of 3-substituted 1-methylpyridinium compounds two isomeric pyridones are normally formed. Only from the 3-carboxylic acid or the 3-nitro derivative results exclusively the corresponding 6-pyridone.
    Notes: Bei der Hexacyanoferrat(III)-Oxydation 3-substituierter 1-Methyl-pyridiniumverbindungen entstehen normalerweise zwei isomere Pyridone. Lediglich bei dem 3-Carboxy- bzw. dem 3-Nitro-Derivat resultiert ausschließlich das entsprechende Pyridon-(6).
    Additional Material: 2 Ill.
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